EP1181059B1 - Competitive chemiluminescent assay for cyclic nucleotide monophosphates - Google Patents

Competitive chemiluminescent assay for cyclic nucleotide monophosphates Download PDF

Info

Publication number
EP1181059B1
EP1181059B1 EP00930260A EP00930260A EP1181059B1 EP 1181059 B1 EP1181059 B1 EP 1181059B1 EP 00930260 A EP00930260 A EP 00930260A EP 00930260 A EP00930260 A EP 00930260A EP 1181059 B1 EP1181059 B1 EP 1181059B1
Authority
EP
European Patent Office
Prior art keywords
cyclic nucleotide
kit
camp
antibody
cyclic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP00930260A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP1181059A1 (en
EP1181059A4 (en
Inventor
Irena Y. Bronstein
Anthony C. Chiulli
Michelle A. J. Palmer
John C. Voyta
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Life Technologies Corp
Original Assignee
Life Technologies Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Life Technologies Corp filed Critical Life Technologies Corp
Priority to EP20100158650 priority Critical patent/EP2213311B1/en
Publication of EP1181059A1 publication Critical patent/EP1181059A1/en
Publication of EP1181059A4 publication Critical patent/EP1181059A4/en
Application granted granted Critical
Publication of EP1181059B1 publication Critical patent/EP1181059B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56966—Animal cells
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/5308—Immunoassay; Biospecific binding assay; Materials therefor for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites

Definitions

  • This invention pertains to a competitive chemiluminescent assay for the detection of the presence of cyclic nucleotide monophosphates.
  • the cyclic nucleotide phosphates appear only as monophosphates, due to chemical structure considerations.
  • cyclic adenosine monophosphate is perhaps the most widely known, implicated as a primary or secondary messenger in a variety of cellular, intracellular and extracellular pathways.
  • This invention takes advantage of the high sensitivity of chemiluminescent 1,2-dioxetane reagents to overcome sensitivity and dynamic range problems encountered in the prior art.
  • cAMP is only the best known of the cyclic nucleotides. In general, cyclic nucleotides appear as monophosphates. Guanosine monophosphate (cGMP), uridine monophosphate (cUMP) and cytidine monophosphate (cCMP) may all importantly bear on a wide variety of hormonal functions and intercellular interactions, that may be desirably measured. cAMP is the most studied of these "messenger" cyclic nucleotides.
  • Assays including competitive ELISA assays, for cAMP are known.
  • a widely reported assay is available from Assay Design, and is a colorometric assay.
  • Other immunoassay products are available from Amersham Med-Physics, Inc. (a radioimmunoassay) as well as IGEN and NEN.
  • the Assay Design embodiment employs assay kits (also available under the mark Biomol) in a classic example of a competitive ELISA assay, in which the strength of the signal is inversely proportional to the concentration of the cyclic nucleotide present.
  • the kit from Biomol is for measurement of light absorption.
  • a fluorescent assay kit is available from Perseptive Biosystems.
  • U.S. 5,856,522 discloses an optically detectable assay method using 1,2- dioxetanes to determine the concentration of a particular substance in a sample. The assay can be used to detect nucleic acids.
  • U.S. 5,739,001 discloses an assay for cAMP by using a plate coated with anti cAMP antibody.
  • U.S. 4,115,538 discloses an assay for assaying cAMP or cGMP using succinylating reagents and anti cAMP antibodies.
  • U.S. 5,399,500 describes solid phase immunoassays using antibody coated substrates suitable for use in competitive assays.
  • U.S. 5,654,154 discloses a DNA assay where the target is bound by a DNA probe with an enzyme linked thereto, the enzyme triggering dioxetane by decomposition.
  • Y 1 , Y 2 and X are variously electron-active moieties, in that they are either electron donating or electron withdrawing.
  • exemplary groups include halogens, particularly chlorine, alkoxies, particularly methoxy, amine, alkyl, etc. In the alternative, these groups are hydrogen. Any one or more of Y 1 , Y 2 or X may be other than hydrogen, or they may all be hydrogen.
  • Substituent R is an alkyl, aralkyl, cyclic alkyl, heteroalkyl comprising an O N, P or S moiety, in general of less than 20 carbon atoms. Desirably, R is alkyl.
  • R may be substituted with groups intended to enhance solubility as well as reactivity, which may include halogen substituents such as one or more fluorine atoms, carboxy (COO) substituents, sulfoxy substituents, etc. The same substituents to enhance solubility may also be present on Y 1 , Y 2 or X.
  • Ar is an aryl moiety, typically phenyl or naphthyl, most preferably phenyl.
  • Z is a moiety which includes a bond which is cleaved by an enzyme, which, when cleaved, leaves either O or N attached to the aryl moiety. This anion destabilizes the dioxetane, leading to its decomposition.
  • Z is a phosphate moiety, preferably disodium phosphate.
  • Dioxetanes of this type are disclosed in U.S. Patents 4,962,192 ; 4,931,569 ; 5,112,960 ; 5,145,772 and 5,654,154 , as well as a variety of others.
  • an enzyme-triggerable dioxetane such as 3-(4-methoxyspiro[1,2-dioxetane-3, 2'-tricyclo[3.3.1.1 3.7 ]decan-4-phenylphosphate and its salts (AMPPD) is a highly effective reporter molecule of this type. Derivitisation of this "unsubstituted" 1,2-dioxetane with substituents on the adamantyl ring, such as a chlorine atom (CSPD) can dramatically improve performance.
  • AMPPD enzyme-triggerable dioxetane
  • these dioxetanes may be combined with energy accepting fluorescent molecules, such as fluorescein, such that the energy released by the dioxetane on decomposition is transferred to the fluorescent receiver, the fluorescence being detected.
  • the assay of this invention is particularly suited for chemiluminescent emission.
  • a microtiter well or similar "reaction chamber” is coated with a capture antibody, which is exemplified by goat anti-rabbit IgG (available from a wide variety of sources, including American Qualex).
  • a conjugate of cAMP and alkaline phosphatase is prepared and added to the well with an antibody for cAMP (or other cyclic nucleotide) and the sample to be inspected (or standard).
  • the reaction mixture is incubated, and washed.
  • an alkaline phosphatase-triggerable 1,2-dioxetane such as CSPD
  • an enhancer such as poly(vinylbenzyltributyl ammonium chloride) or other enhancement agent.
  • the dioxetane is incubated, and the reaction chamber inspected, preferably with a luminometer, or some other type of light-sensitive device, for chemiluminescent signal. The stronger the signal, the lower the cyclic nucleotide concentration in the sample.
  • the assay protocol of this invention resembles other competitive immunoassays, and provides an inverse relationship between strength of signal detected and cyclic nucleotide concentration.
  • the invention is generically applicable to the cyclic nucleotides, including cAMP, cGMP, cCMP, cUNT, cIMP and cTMP, cAMP and cGMP, which frequently appear in a tandem, inverse relationship in a wide variety of biophysical pathways, receive the most attention.
  • cAMP is clearly the most well studied and characterized of the cyclic nucleotides, and accordingly, this invention is exemplified using cAMP and cAMP detection reagents.
  • the substitution of reagents, in particular, primary antibodies, preferably monoclonal antibodies, for the other cyclic nucleotides is straight forward and easily arrived at by one of skill in the art, given the disclosure herein.
  • This invention is also exemplified using CSPD, where, in the general Formula I given above, the adamantyl group is substituted with 1 chlorine atom, X is hydrogen, R is methyl and Z is phosphate.
  • This invention is also exemplified using an enhancement agent, commercially available from Tropix, Inc.
  • an enhancement agent poly(vinylbenzyltributylammonium chloride) is selected.
  • An enhancement agent is preferred, but not required for the practice of the invention.
  • Other quaternary onium polymers, as well as hydrophobic macromolecules such as large proteins, including bovine serum albumin may be similarly employed.
  • the wells of conventional microtiter plates, or similar reaction chambers are first coated with capture antibody.
  • the capture antibody is a goat anti-rabbit antibody.
  • the wells of the plates are coated with a preparation of the capture antibody, incubated over night, and then washed. To avoid non-specific binding, the rest of the plate may be treated, so as to suppress any interaction therewith. Accordingly, after washing, each plate is treated with SuperBlock blocking buffer (available from Pierce) or similar agent. The plate is thereafter dried. This process is reflected in Figure 1 .
  • the prepared plates are now ready to perform as reaction chambers, or wells, for the competitive assay.
  • the source of cAMP is either standards prepared to specific dilutions, in order to establish standardized values, or cells that have been subjected to some type of stimulus, and are then lysed, so as to provide sample material for inspection.
  • the cell lysate or cAMP standard is added to the wells, together with a conjugate of cAMP and alkaline phosphatase, described herein below.
  • Final addition to the reaction mixture is the primary antibody, an antibody for cAMP. Both polyclonal and monoclonal antibodies are available against cAMP. Either may be used effectively. Rabbit anti-cAMP antibodies are available from Zymed Laboratories, Inc. as well Immunogen.
  • the reactants are mixed in the coated well, and then incubated to insure adequate antibody binding. Typically, incubation is at room temperature for a period of about one hour. Subsequently, the incubated reaction mixture is washed repeatedly, with a wash buffer which may be 0.05 M carbonate bicarbonate and 0.05% Tween-20 at a pH of about 8.0-11.0, an exemplary value being about 9.6. While Applicants do not wish to be bound by this theory, the alkaline character of the wash buffer may improve alkaline phosphatase performance.
  • the assay buffer itself is BSA (0.02%) with sodium acetate (0.05 molar) at a pH convenient for the assay, between about 5.5 and 6.0, preferably about 5.8.
  • the dioxetane After washing, the dioxetane, with the enhancer, if any, is added. A further incubation, to permit a glow discharge from the chemiluminescent dioxetane to reach a constant level, approximately 30 minutes at room temperature, follows, and then the chemiluminescent signal is read in a detection device, such as the Tropix 717 or North Star luminometer detection device (CCD).
  • a detection device such as the Tropix 717 or North Star luminometer detection device (CCD).
  • the assay protocol itself is set forth in Figure 2 .
  • This assay is suitable for use in a wide variety of conditions.
  • the heightened sensitivity, and broadened dynamic range makes application consistent with a wide variety of variables.
  • the samples assayed according to this invention can be obtained by lysing mammalian adherent and non-adherent cell lines. Optimal performance can be achieved across a wide range of cell densities, ranging from 1,000 - 100,000 cells per well, depending on cell type in a 96-well plate. Other plates with a higher number of wells, may be used.
  • the use of luminometers to detect the chemiluminescent signal (light emission) is recommended. If a luminometer is used, an appropriate measure is 1 second per well.
  • a scintillation counter such as that available under the trademark Top Count may be used a substitute for a luminometer. Sensitivity may be reduced, and it is necessary to turn off the coincident circuit to measure chemiluminescence directly.
  • the "competitive" basis of the assay is the use of a conjugate of cAMP and alkaline phosphatase (cAMP-AP conjugate). It is the alkaline phosphatase of this cAMP-AP conjugate, captured by the antibody specific for cAMP, that cleaves the alkaline phosphatase-cleavable dioxetane.
  • cAMP-AP conjugate conjugate of cAMP and alkaline phosphatase
  • the conjugate is straight forward, and comprises combining NHS activated cAMP with alkaline phosphatase (in a ratio of 4 moles activated cAMP to 1 mole AP). This preparation is reflected in Figure 4 .
  • Sensitivity and dynamic range for a variety of cAMP detection assays have been published. Sensitivity and dynamic range of a variety of detection systems are set forth in Figure 6 . It is clear that the unexpected improvements in sensitivity and dynamic range obtained by combining dioxetane chemiluminescent technology with cAMP-specific immunoassay techniques has led to an unexpectedly superior performance, even in the absence of acetylation.
  • the cyclic AMP chemiluminescent assay of the invention is preferably detected by the luminometer.
  • Two exemplary luminometers are compared in Figure 7 , TR717 verses Orion CCD. Both give the improved performance advantangeously provided by this invention.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Chemical & Material Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Cell Biology (AREA)
  • Food Science & Technology (AREA)
  • Physics & Mathematics (AREA)
  • Biotechnology (AREA)
  • Pathology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • General Physics & Mathematics (AREA)
  • Medicinal Chemistry (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Zoology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Saccharide Compounds (AREA)
EP00930260A 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates Expired - Lifetime EP1181059B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP20100158650 EP2213311B1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US307797 1999-05-10
US09/307,797 US6686171B2 (en) 1999-05-10 1999-05-10 Competitive chemiluminescent assay for cyclic nucleotide monophosphates
PCT/US2000/011726 WO2000067804A1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates

Related Child Applications (2)

Application Number Title Priority Date Filing Date
EP20100158650 Division EP2213311B1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates
EP10158650.1 Division-Into 2010-03-31

Publications (3)

Publication Number Publication Date
EP1181059A1 EP1181059A1 (en) 2002-02-27
EP1181059A4 EP1181059A4 (en) 2005-01-12
EP1181059B1 true EP1181059B1 (en) 2010-08-11

Family

ID=23191203

Family Applications (2)

Application Number Title Priority Date Filing Date
EP00930260A Expired - Lifetime EP1181059B1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates
EP20100158650 Expired - Lifetime EP2213311B1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP20100158650 Expired - Lifetime EP2213311B1 (en) 1999-05-10 2000-05-02 Competitive chemiluminescent assay for cyclic nucleotide monophosphates

Country Status (8)

Country Link
US (1) US6686171B2 (enExample)
EP (2) EP1181059B1 (enExample)
JP (1) JP5021120B2 (enExample)
AT (1) ATE477001T1 (enExample)
AU (1) AU4811400A (enExample)
CA (1) CA2373873A1 (enExample)
DE (1) DE60044809D1 (enExample)
WO (1) WO2000067804A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6794156B2 (en) * 1999-05-10 2004-09-21 Applera Corporation Cell growth, induction and lysis in an antibody-coated microplate for use in an ELISA
US8168592B2 (en) * 2005-10-21 2012-05-01 Amgen Inc. CGRP peptide antagonists and conjugates
ES2452318T3 (es) 2006-12-21 2014-03-31 F. Hoffmann-La Roche Ag Método para la detección de AMPc y GMPc
US20130017197A1 (en) * 2010-03-31 2013-01-17 Universite De Geneve Stabilized antibody preparations and uses thereof
US10767234B2 (en) 2017-03-31 2020-09-08 Regents Of The University Of Minnesota Methods for microbial screening and identification of targets of interest

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5825980B2 (ja) * 1976-02-12 1983-05-31 ヤマサ醤油株式会社 サイクリックヌクレオチドの定量法
JPS57146594A (en) * 1981-03-06 1982-09-10 Yamasa Shoyu Co Ltd Preparation of anticyclic nucleotide antibody
US4962192A (en) 1986-07-17 1990-10-09 Board Of Governors Of Wayne State University Chemiluminescent 1,2-dioxetane compounds
CA1340590C (en) * 1986-07-24 1999-06-08 John C. Voyta Chemiluminescence enhancement
US5112960A (en) 1989-07-17 1992-05-12 Bronstein Irena Y Chemiluminescent 3-(substituted adamant-2'-ylidene) 1,2-dioxetanes
US5856522A (en) 1995-05-04 1999-01-05 Tropix, Inc. Method of using synthesis of 1,2-dioxetanes and kits therefore
US5089424A (en) * 1988-06-14 1992-02-18 Abbott Laboratories Method and apparatus for heterogeneous chemiluminescence assay
US4931569A (en) 1988-09-14 1990-06-05 Tropix, Inc. Purification of stable water-soluble dioxetanes
JPH05504683A (ja) * 1989-12-20 1993-07-22 ニコルス　インスティテュート　ダイアグノスティックス 組み換えチロトロピン受容体
US5547836A (en) * 1990-08-30 1996-08-20 Tropix, Inc. Enhancement of chemiluminescent assays
JP2999810B2 (ja) * 1990-09-10 2000-01-17 トロピックス・インコーポレーテッド １，２−ジオキセタン化合物
DE69210225T2 (de) * 1991-02-14 1996-12-05 Baxter Int Herstellungsverfahren für biegsame biologische Gewebeverpflanzungsmaterialen
US5399500A (en) * 1992-06-26 1995-03-21 Becton Dickinson And Company Two step process for coating of antibodies to a solid phase
DE69430322T2 (de) * 1993-12-23 2002-11-14 Tropix, Inc. Chemilumineszenz-assay mittels energietransfer
US5589344A (en) * 1994-06-15 1996-12-31 Johnson & Johnson Clinical Diagnostics, Inc. Test kit and method for competitive specific binding assay
US5739001A (en) * 1996-10-29 1998-04-14 E. I. Du Pont De Nemours And Company Solid phase cell-based assay

Also Published As

Publication number Publication date
AU4811400A (en) 2000-11-21
US20020115123A1 (en) 2002-08-22
US6686171B2 (en) 2004-02-03
EP1181059A1 (en) 2002-02-27
WO2000067804A1 (en) 2000-11-16
DE60044809D1 (de) 2010-09-23
EP2213311A1 (en) 2010-08-04
ATE477001T1 (de) 2010-08-15
EP2213311B1 (en) 2015-04-22
CA2373873A1 (en) 2000-11-16
JP5021120B2 (ja) 2012-09-05
EP1181059A4 (en) 2005-01-12
JP2002544493A (ja) 2002-12-24

Similar Documents

Publication Publication Date Title
US5753436A (en) Chemiluminescent energy transfer assays
US6180340B1 (en) Extended dynamic range assays
EP0446245B1 (en) Electrochemiluminescent assays
US6689576B2 (en) Chemiluminescent assay
US12372474B2 (en) Branched-chain amines in electrochemiluminescence detection
JPH08240590A (ja) 特異的結合アッセイ用試薬およびそのキット
US20130224758A1 (en) Use of signal enhancing compounds in electrochemiluminescence detection
EP1181059B1 (en) Competitive chemiluminescent assay for cyclic nucleotide monophosphates
EP1501553B1 (en) Cell growth, induction and lysis in an antibody-coated microplate for use in an elisa
JPH10511460A (ja) 被験サンプル中の複数分析物の時差式検出方法
AU704940B2 (en) Chemiluminescent energy transfer assays
EP1071954A1 (en) Comb-like solid phase for measuring analytes
Bhayana et al. A double monoclonal time-resolved immunofluorometric assay of carcinoembryonic antigen in serum
EP1177443A2 (en) A method for measuring biomolecules
Hsu Department of Pathology and Laboratory Medicine University of Texas Health Science Center
AU4344799A (en) chemiluminescent energy transfer assays

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20011210

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: APPLERA CORPORATION

A4 Supplementary search report drawn up and despatched

Effective date: 20041125

17Q First examination report despatched

Effective date: 20071220

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: LIFE TECHNOLOGIES CORPORATION

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: LIFE TECHNOLOGIES CORPORATION

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 60044809

Country of ref document: DE

Date of ref document: 20100923

Kind code of ref document: P

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20100811

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20101213

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20101112

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100811

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20101122

26N No opposition filed

Effective date: 20110512

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 60044809

Country of ref document: DE

Effective date: 20110512

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110531

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110531

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110531

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110502

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20110502

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 17

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 18

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 19

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20190416

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20190410

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20190515

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 60044809

Country of ref document: DE

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20200501

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20200501